{"title":"Clinical significance of a novel inflammatory-nutritional index in glaucoma severity evaluation.","authors":"Xiao Xiao, Yanping Gao, Gao Zhang, Zuo Wang, An Li, Donghua Liu, Jing Fu, Wenbo Xiu, Chang Lu, Jinxia Wang, Xiong Zhu, Yang Chen, Lingling Chen, Bolin Deng, Ping Shuai, Chong He, Fang Lu","doi":"10.17305/bb.2025.12374","DOIUrl":null,"url":null,"abstract":"<p><p>This study investigated the association between glaucoma and serum albumin (Alb), lymphocyte percentage (LYMPH%), and their combined index (LAP = LYMPH% × Alb), to evaluate their potential as biomarkers for systemic inflammation and disease progression in glaucoma. We enrolled 161 glaucoma patients and 181 healthy controls. Serum Alb and LYMPH% were measured using standard blood biochemistry and routine tests, and LAP was calculated accordingly. Statistical analyses were performed to compare these markers between groups and assess their correlation with disease severity. Both the median serum Alb level and peripheral blood LYMPH% were significantly lower in the glaucoma group compared to controls (Alb: 43.48 g/L vs 44.63 g/L, P < 0.001; LYMPH%: 24.25% vs 29.12%, P < 0.001). Correspondingly, LAP levels were also significantly reduced in glaucoma patients (1053 vs 1298, P < 0.001). Lower LYMPH% and LAP levels were associated with more severe glaucomatous visual impairment (LAP, healthy controls vs glaucoma: AUC = 0.7080, P < 0.001, Max Youden = 0.3621; early vs severe glaucoma: AUC = 0.8061, P < 0.001, Max Youden = 0.5377). In summary, LAP may serve as a supportive biomarker of systemic inflammation in glaucoma. It demonstrates good accuracy in reflecting glaucoma severity and shows potential for monitoring disease progression.</p>","PeriodicalId":72398,"journal":{"name":"Biomolecules & biomedicine","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomolecules & biomedicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17305/bb.2025.12374","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"0","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0
Abstract
This study investigated the association between glaucoma and serum albumin (Alb), lymphocyte percentage (LYMPH%), and their combined index (LAP = LYMPH% × Alb), to evaluate their potential as biomarkers for systemic inflammation and disease progression in glaucoma. We enrolled 161 glaucoma patients and 181 healthy controls. Serum Alb and LYMPH% were measured using standard blood biochemistry and routine tests, and LAP was calculated accordingly. Statistical analyses were performed to compare these markers between groups and assess their correlation with disease severity. Both the median serum Alb level and peripheral blood LYMPH% were significantly lower in the glaucoma group compared to controls (Alb: 43.48 g/L vs 44.63 g/L, P < 0.001; LYMPH%: 24.25% vs 29.12%, P < 0.001). Correspondingly, LAP levels were also significantly reduced in glaucoma patients (1053 vs 1298, P < 0.001). Lower LYMPH% and LAP levels were associated with more severe glaucomatous visual impairment (LAP, healthy controls vs glaucoma: AUC = 0.7080, P < 0.001, Max Youden = 0.3621; early vs severe glaucoma: AUC = 0.8061, P < 0.001, Max Youden = 0.5377). In summary, LAP may serve as a supportive biomarker of systemic inflammation in glaucoma. It demonstrates good accuracy in reflecting glaucoma severity and shows potential for monitoring disease progression.
本研究探讨了青光眼与血清白蛋白(Alb)、淋巴细胞百分比(LYMPH%)及其联合指数(LAP = LYMPH% × Alb)之间的关系,以评估它们作为青光眼系统性炎症和疾病进展的生物标志物的潜力。我们招募了161名青光眼患者和181名健康对照者。采用标准血生化和常规检查测定血清Alb和LYMPH%,并计算LAP。进行统计分析比较各组之间的这些标记物,并评估它们与疾病严重程度的相关性。青光眼组中位血清Alb水平和外周血LYMPH%均显著低于对照组(Alb: 43.48 g/L vs 44.63 g/L, P < 0.001;淋巴%:24.25% vs 29.12%, P < 0.001)。相应地,青光眼患者的LAP水平也显著降低(1053 vs 1298, P < 0.001)。较低的淋巴%和LAP水平与更严重的青光眼视力损害相关(LAP,健康对照与青光眼:AUC = 0.7080, P < 0.001, Max Youden = 0.3621;早期青光眼vs重度青光眼:AUC = 0.8061, P < 0.001, Max Youden = 0.5377)。综上所述,LAP可作为青光眼全身性炎症的支持性生物标志物。它在反映青光眼严重程度方面显示出良好的准确性,并显示出监测疾病进展的潜力。